Zlotogora J, Carrasquillo MM, Barges S, Shalev SA, Hujerat Y, Chakravarti A: High incidence of deafness from three frequent connexin 26 mutations in an isolated community. Genet Testing 10:40-43, 2006. PMID 16545002.
Young JH, Chang Y-PC, Kim J, Chretien J-P, Klag MJ, Levine MA, Ruff CB, Chakravarti A: Differential susceptibility to hypertension is due to selection during the Out-of-Africa expansion. PloS Genet 1:731-738, 2005. PMID 16429165. PMC1342636.
Gu CC, Chang Y-P C, Hunt S, Schwander K, Arnett D, Djousse L, Heiss G, Oberman A, Lalouel J- M, Province M, Chakravarti A, Rao DC: Haplotype Association Analysis of AGT Variants with Hypertension-related Traits: The HyperGEN Study. Hum Hered 60:164-176, 2005. PMID 16352906.
Grice E, Rochelle ES, Green ED, Chakravarti A, McCallion AS: Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer. Hum Mol Genet 14:3837-3845, 2005. PMID 16269442.
Armanios M, Chen J-L, Chang Y-P, Brodsky RA, Hawkins A, Griffin CA, Eshleman J, Cohen AR, Chakravarti A, Hamosh A, Greider C: Haploinsufficiency of hTERT Leads to Anticipation in Autosomal Dominant Dyskeratosis Congenita. Proc Natl Acad Sci (USA) 102:15960-15964, 2005. PMID 16247010. PMC1276104.
Rasmussen-Torvik LJ, North KE, Gu CC, Lewis CE, Wilk JB, Chakravarti A, Chang Y-P C, Miller MB, Li N, Devereux RB, Arnett DK: A population association study of angiotensinogen polymorphisms and haplotypes with left ventricular phenotypes. Hypertension 46:1294-1299, 2005. PMID 16286570.
The International HapMap Consortium: A Haplotype Map of the Human Genome. Nature 437:1299-1320, 2005. PMID 16255080. PMC1880871.
Maitra A, Arking DE, Shivapurkar N, Ikeda M, Stastny V, Kassauei K, Sui G, Cutler DJ, Ying Liu, Brimble SN, Noaksson K, Hyllner J, Schulz TC, Zeng X, Freed WJ, Colman A, Sartipy P, Matsui S-I, Carpenter M, Gazdar AF, Rao M, Chakravarti A: Genomic Alterations in Cultured Human Embryonic Stem Cells. Nat Genet 37:1099-1103, 2005. PMID 16142235.
Zlotogora J, Hujerat Y, Zalman L, Barges S, Filon D, Koren A, Shalev SA, Chakravarti A: Origin and Expansion of Four Different Beta Globin Mutations in a Single Arab Village. Amer J Hum Biol 17:659-661, 2005. PMID 16136542.
Mitchell AA, Chakravarti A, Cutler DJ: On the probability that a novel variant is a disease- causing mutation. Genome Res 15:960-966, 2005. PMID 15965029. PMC1172040.